北京大学学报(医学版) ›› 2022, Vol. 54 ›› Issue (3): 412-420. doi: 10.19723/j.issn.1671-167X.2022.03.004
杨若彤,王梦莹,李春男,于欢,王小文,吴俊慧,王斯悦,王伽婷,陈大方,吴涛,胡永华*()
Ruo-tong YANG,Meng-ying WANG,Chun-nan LI,Huan YU,Xiao-wen WANG,Jun-hui WU,Si-yue WANG,Jia-ting WANG,Da-fang CHEN,Tao WU,Yong-hua HU*()
摘要:
目的: 探讨睡眠行为(睡眠时长、睡眠效率、入睡时间)和全基因组关联研究(genome-wide association studies, GWAS)提示阳性缺血性脑卒中(ischemic stroke, IS)基因位点与IS风险的关联,以及睡眠-基因交互作用与IS风险的关联。方法: 基于北京市房山家系队列,在基线对所有研究对象进行问卷调查、体格检查、血生化检测和基因型检测。采用多因素广义线性模型分析睡眠、基因与IS的关联。结果: 共纳入研究对象4 648人,平均年龄(58.5±8.7)岁,其中IS患者有1 316人。相比于非患者,IS患者睡眠时长≥9 h、睡眠效率 < 80%及入睡时间早于22:00占比更高(P均 < 0.05)。多因素广义线性模型下,未见睡眠时长与IS风险的线性关联(OR=1.04,95%CI:0.99~1.10,P=0.085)。睡眠效率与IS风险呈线性负相关(OR=0.18,95%CI:0.06~0.53,P=0.002);相比于睡眠效率≥80%,睡眠效率 < 80%的IS风险为其1.47倍(95%CI:1.03~2.10,P=0.033)。相较于在22:00—22:59入睡,入睡时间早于22:00的IS风险是其1.26倍(95%CI:1.04~1.52,P=0.017)。多因素模型发现ABO基因上rs579459位点与入睡时间存在交互作用(P交互=0.040),rs579459致病等位基因T个数为2时,相比于入睡时间22:00—22:59,早于22:00入睡者IS风险显著升高,为其1.56倍(95%CI:1.20~2.04,P=0.001),而致病等位基因个数为0或1时无显著关联。仅调整性别、年龄、家系的模型中,睡眠时长与PITX2基因上rs2634074致病等位基因T的个数对IS存在交互作用(P交互=0.033)。结论: 睡眠效率降低与IS风险增高有关,入睡时间早于22:00与较高的IS风险相关。入睡时间与ABO基因上rs579459和IS风险存在交互作用;睡眠时长与PITX2基因上rs2634074和IS风险可能存在潜在的交互作用。
中图分类号:
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